Canonical Question
Pharmaceutics
Master answer
Enantiomers
- Molecules which have the same bond structure but are mirror images of each other.
- These molecules rotate light in opposite directions:
- (S)-(+)-naproxen is used to treat arthritis pain
- (R)-(–)-naproxen causes liver poisoning with no analgesic effect.
- (S)-(+)-warfarin, metabolised by CYP2C9, 3-5 times more potent
- (R)-(–)-warfarin, metabolised by CYP2C19, CYP1A2, CYP3A4
- These are isomers which share pharmachemical properties (boiling point, density…) and chemical formula but different 3-D structural arrangement.
- If action depends on pharacochemical properties then it is shared between enantomes
- If action depends on binding to specific sites then it can be markedly different between enantomers.
Enantomers are a subclass of Sterioisomers which are molecules with the same bond structure, different 3D arrangement.
- Sterioisomers have a singel chiral center and can be either:
- Geometric
- Optical or enantomeric
- Diastereoisomers have more than one chiral center and can be either:
- Geometric
- Optical non-enantomeric
Gladwin 2016
Exam appearances
| Exam | Exact wording | Relationship | Success |
|---|---|---|---|
| 2012B Q20 | What are drug enantiomers? (20% of marks). Explain the clinical relevance of enantiomerism (60% of marks). Give a clinically relevant example (20% of marks). | historical_member | — |